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Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2.
Hum Mol Genet. 2015 Feb 1;24(3):659-69. doi: 10.1093/hmg/ddu486. Epub 2014 Sep 25.
Hum Mol Genet. 2015.
PMID: 25256356
Free PMC article.
Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity.
Sacconi S, Camaño P, de Greef JC, Lemmers RJ, Salviati L, Boileau P, Lopez de Munain Arregui A, van der Maarel SM, Desnuelle C.
Sacconi S, et al. Among authors: lopez de munain arregui a.
J Med Genet. 2012 Jan;49(1):41-6. doi: 10.1136/jmedgenet-2011-100101. Epub 2011 Oct 7.
J Med Genet. 2012.
PMID: 21984748
Free PMC article.
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Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease.
Gutiérrez Gutiérrez G, Díaz-Manera J, Almendrote M, Azriel S, Eulalio Bárcena J, Cabezudo García P, Camacho Salas A, Casanova Rodríguez C, Cobo AM, Díaz Guardiola P, Fernández-Torrón R, Gallano Petit MP, García Pavía P, Gómez Gallego M, Gutiérrez Martínez AJ, Jericó I, Kapetanovic García S, López de Munaín Arregui A, Martorell L, Morís de la Tassa G, Moreno Zabaleta R, Muñoz-Blanco JL, Olivar Roldán J, Pascual Pascual SI, Peinado Peinado R, Pérez H, Poza Aldea JJ, Rabasa M, Ramos A, Rosado Bartolomé A, Rubio Pérez MÁ, Urtizberea JA, Zapata-Wainberg G, Gutiérrez-Rivas E.
Gutiérrez Gutiérrez G, et al. Among authors: lopez de munain arregui a.
Med Clin (Barc). 2019 Jul 19;153(2):82.e1-82.e17. doi: 10.1016/j.medcli.2018.10.028. Epub 2019 Jan 24.
Med Clin (Barc). 2019.
PMID: 30685181
English, Spanish.
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Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease.
Gutiérrez Gutiérrez G, Díaz-Manera J, Almendrote M, Azriel S, Eulalio Bárcena J, Cabezudo García P, Camacho Salas A, Casanova Rodríguez C, Cobo AM, Díaz Guardiola P, Fernández-Torrón R, Gallano Petit MP, García Pavía P, Gómez Gallego M, Gutiérrez Martínez AJ, Jericó I, Kapetanovic García S, López de Munaín Arregui A, Martorell L, Morís de la Tassa G, Moreno Zabaleta R, Muñoz-Blanco JL, Olivar Roldán J, Pascual Pascual SI, Peinado Peinado R, Pérez H, Poza Aldea JJ, Rabasa M, Ramos A, Rosado Bartolomé A, Rubio Pérez MÁ, Urtizberea JA, Zapata-Wainberg G, Gutiérrez-Rivas E.
Gutiérrez Gutiérrez G, et al. Among authors: lopez de munain arregui a.
Neurologia (Engl Ed). 2020 Apr;35(3):185-206. doi: 10.1016/j.nrl.2019.01.001. Epub 2019 Apr 16.
Neurologia (Engl Ed). 2020.
PMID: 31003788
Free article.
English, Spanish.
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Risk factors associated with COVID-19 infection and mortality in nursing homes.
Beobide Telleria I, Ferro Uriguen A, Laso Lucas E, Sannino Menicucci C, Enriquez Barroso M, López de Munain Arregui A.
Beobide Telleria I, et al. Among authors: lopez de munain arregui a.
Aten Primaria. 2022 Oct;54(10):102463. doi: 10.1016/j.aprim.2022.102463. Epub 2022 Sep 6.
Aten Primaria. 2022.
PMID: 36148713
Free PMC article.
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LRP10 in α-synucleinopathies.
Kia DA, Sabir MS, Ahmed S, Trinh J, Bandres-Ciga S; International Parkinson's Disease Genomics Consortium.
Kia DA, et al.
Lancet Neurol. 2018 Dec;17(12):1032. doi: 10.1016/S1474-4422(18)30401-0. Epub 2018 Nov 13.
Lancet Neurol. 2018.
PMID: 30507383
No abstract available.
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Myasthenia gravis: descriptive analysis of life-threatening events in a recent nationwide registry.
Ramos-Fransi A, Rojas-García R, Segovia S, Márquez-Infante C, Pardo J, Coll-Cantí J, Jericó I, Illa I; Myasthenia NMD-ES Study Group.
Ramos-Fransi A, et al.
Eur J Neurol. 2015 Jul;22(7):1056-61. doi: 10.1111/ene.12703. Epub 2015 Apr 6.
Eur J Neurol. 2015.
PMID: 25847221
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